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Targeting genetic lesions in esophageal cancer

机译:靶向食道癌的遗传病变

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As one of the most aggressive cancers, esophageal squamous cell carcinoma (ESCC) is the sixth leading cause of cancer deaths worldwide and particularly common in Asia. Over the decades, the clinical management of ESCC patients has barely advanced; and the overall survival remains poor, largely because its molecular basis, especially the genomic abnormalities, is obscure, and no targeted therapy has been established. Very recently, we and Song et al. have comprehensively characterized the genomic landscape of a total of approximately 300 ESCCs with whole-genome/ exome sequencing, targeted sequencing, and copy number profiling, providing an important molecular foundation for understanding esophageal tumors and developing therapeutic targets.
机译:食道鳞状细胞癌(ESCC)作为最具侵略性的癌症之一,是全球导致癌症死亡的第六大主要原因,在亚洲尤为常见。几十年来,ESCC患者的临床管理几乎没有进展。而且总体生存率仍然很差,主要是因为其分子基础,尤其是基因组异常尚不清楚,因此尚未建立靶向治疗方法。最近,我们和宋等人。通过全基因组/外显子组测序,靶向测序和拷贝数分析,全面鉴定了总共约300个ESCC的基因组格局,为了解食管肿瘤和制定治疗靶点提供了重要的分子基础。

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